CA2670055C - Waterborne, radiation-curable coating compositions and related methods - Google Patents

Waterborne, radiation-curable coating compositions and related methods Download PDF

Info

Publication number: CA2670055C
Authority: CA; Canada
Prior art keywords: coating composition; polymer; percent; present; composition
Prior art date: 2006-11-21
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Fee Related

Application number

CA2670055A

Other languages

English (en)

French (fr)

Other versions

CA2670055A1 (en

Inventor

M. Lisa Perrine

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

PPG Industries Ohio Inc

Original Assignee

PPG Industries Ohio Inc

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2006-11-21

Filing date

2007-11-07

Publication date

2012-05-15

2007-11-07 Application filed by PPG Industries Ohio Inc filed Critical PPG Industries Ohio Inc

2008-05-29 Publication of CA2670055A1 publication Critical patent/CA2670055A1/en

2012-05-15 Application granted granted Critical

2012-05-15 Publication of CA2670055C publication Critical patent/CA2670055C/en

Status Expired - Fee Related legal-status Critical Current

2027-11-07 Anticipated expiration legal-status Critical

Links

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239000011777 magnesium Substances 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical group OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
238000005259 measurement Methods 0.000 description 1
JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
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ZWRDBWDXRLPESY-UHFFFAOYSA-N n-benzyl-n-ethylethanamine Chemical compound CCN(CC)CC1=CC=CC=C1 ZWRDBWDXRLPESY-UHFFFAOYSA-N 0.000 description 1
WGESLFUSXZBFQF-UHFFFAOYSA-N n-methyl-n-prop-2-enylprop-2-en-1-amine Chemical compound C=CCN(C)CC=C WGESLFUSXZBFQF-UHFFFAOYSA-N 0.000 description 1
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229920005615 natural polymer Polymers 0.000 description 1
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230000000379 polymerizing effect Effects 0.000 description 1
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229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
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229920002689 polyvinyl acetate Polymers 0.000 description 1
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LLBIOIRWAYBCKK-UHFFFAOYSA-N pyranthrene-8,16-dione Chemical compound C12=CC=CC=C2C(=O)C2=CC=C3C=C4C5=CC=CC=C5C(=O)C5=C4C4=C3C2=C1C=C4C=C5 LLBIOIRWAYBCKK-UHFFFAOYSA-N 0.000 description 1
239000010453 quartz Substances 0.000 description 1
IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
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GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
239000004753 textile Substances 0.000 description 1
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JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
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239000004408 titanium dioxide Substances 0.000 description 1
150000003613 toluenes Chemical class 0.000 description 1
ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
VPYJNCGUESNPMV-UHFFFAOYSA-N triallylamine Chemical compound C=CCN(CC=C)CC=C VPYJNCGUESNPMV-UHFFFAOYSA-N 0.000 description 1
125000005627 triarylcarbonium group Chemical group 0.000 description 1
238000001771 vacuum deposition Methods 0.000 description 1
LSGOVYNHVSXFFJ-UHFFFAOYSA-N vanadate(3-) Chemical compound [O-][V]([O-])([O-])=O LSGOVYNHVSXFFJ-UHFFFAOYSA-N 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000002025 wood fiber Substances 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/44—Preparation of metal salts or ammonium salts
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
- C08F265/04—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of esters
- C08F265/06—Polymerisation of acrylate or methacrylate esters on to polymers thereof
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/101—Esters; Ether-esters of monocarboxylic acids
- C08K5/103—Esters; Ether-esters of monocarboxylic acids with polyalcohols
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/08—Homopolymers or copolymers of acrylic acid esters
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
- C09D4/06—Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09D159/00 - C09D187/00
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0025—Crosslinking or vulcanising agents; including accelerators

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
General Chemical & Material Sciences (AREA)
Paints Or Removers (AREA)
Application Of Or Painting With Fluid Materials (AREA)

CA2670055A 2006-11-21 2007-11-07 Waterborne, radiation-curable coating compositions and related methods Expired - Fee Related CA2670055C (en)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
US11/562,069		2006-11-21
US11/562,069 US8138262B2 (en)	2006-11-21	2006-11-21	Waterborne, radiation-curable coating compositions and related methods
PCT/US2007/083892 WO2008063887A2 (en)	2006-11-21	2007-11-07	Waterborne, radiation-curable coating compositions and related methods

Publications (2)

Publication Number	Publication Date
CA2670055A1 CA2670055A1 (en)	2008-05-29
CA2670055C true CA2670055C (en)	2012-05-15

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Application Number	Title	Priority Date	Filing Date
CA2670055A Expired - Fee Related CA2670055C (en)	2006-11-21	2007-11-07	Waterborne, radiation-curable coating compositions and related methods

Country Status (15)

Country	Link
US (2)	US8138262B2 (pl)
EP (2)	EP2527372B1 (pl)
KR (1)	KR101116435B1 (pl)
CN (1)	CN101563370B (pl)
AR (1)	AR064255A1 (pl)
AU (1)	AU2007323973B2 (pl)
BR (1)	BRPI0717662A2 (pl)
CA (1)	CA2670055C (pl)
CL (1)	CL2007003339A1 (pl)
MY (1)	MY145781A (pl)
NO (1)	NO20092204L (pl)
NZ (1)	NZ577082A (pl)
PL (2)	PL2091976T3 (pl)
TW (1)	TWI424032B (pl)
WO (1)	WO2008063887A2 (pl)

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EP1615966B2 (en) *	2003-04-02	2019-10-09	Swimc Llc	Aqueous dispersions and coatings
PL3037488T3 (pl)	2004-10-20	2022-11-14	Swimc Llc	Kompozycje powlekające dla pojemników i sposoby powlekania
JP5247660B2 (ja) *	2009-11-12	2013-07-24	キヤノン株式会社	トナー画像定着方法
EP2749606B1 (en)	2012-12-21	2018-11-21	Rohm and Haas Company	Acrylic dispersions with multi-functional acrylates for UV-cure coatings
US11795937B2 (en)	2020-01-08	2023-10-24	Baker Hughes Oilfield Operations, Llc	Torque monitoring of electrical submersible pump assembly

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4157924A (en)	1978-08-25	1979-06-12	The Dow Chemical Company	Process of applying weldable coating compositions to a metallic substrate
US4186036A (en)	1978-08-25	1980-01-29	The Dow Chemical Company	Weldable coating compositions
JPH02230152A (ja)	1987-06-18	1990-09-12	Napp Syst Usa Inc	感光性樹脂組成物
EP0320873B1 (en) *	1987-12-17	1993-03-31	The B.F. Goodrich Company	An improved process for preparing elastomeric coatings on fibers and compositions of water-dispersed polymers
US5045435A (en) *	1988-11-25	1991-09-03	Armstrong World Industries, Inc.	Water-borne, alkali-developable, photoresist coating compositions and their preparation
JPH07170054A (ja) *	1993-12-14	1995-07-04	Canon Inc	紫外線硬化性組成物、これを用いたパターン形成方法及び配線基板の製造方法
US5530043A (en) *	1994-05-25	1996-06-25	Ppg Industries, Inc.	Low volatile organic content pigment grind composition
IL116255A (en) *	1995-01-05	2004-02-19	Du Pont	High-solids coating composition
WO1996041240A1 (en) *	1995-06-07	1996-12-19	W.R. Grace & Co.-Conn.	Water photoresist emulsions and methods of preparation thereof
JP2002121207A (ja) *	2000-10-16	2002-04-23	Kanegafuchi Chem Ind Co Ltd	組成物とそれを用いた感光性組成物及びカバーレイ
US6875800B2 (en)	2001-06-18	2005-04-05	Ppg Industries Ohio, Inc.	Use of nanoparticulate organic pigments in paints and coatings
US6894086B2 (en)	2001-12-27	2005-05-17	Ppg Industries Ohio, Inc.	Color effect compositions
US20030175437A1 (en) *	2002-03-13	2003-09-18	Masuji Tsuda	Coating film forming method
EP1359173B1 (en) *	2002-04-29	2005-07-06	Dainippon Ink And Chemicals, Inc.	Polymerizable solid compositions
WO2004003074A1 (en) *	2002-05-31	2004-01-08	Cray Valley Iberica	Dual cure emulsions
US7728068B2 (en) *	2003-06-12	2010-06-01	Valspar Sourcing, Inc.	Coating compositions containing reactive diluents and methods
WO2005058995A1 (en) *	2003-12-17	2005-06-30	Dsm Ip Assets B.V.	Stain resistant urethane-vinyl aqueous coating compositions
US7438972B2 (en)	2004-06-24	2008-10-21	Ppg Industries Ohio, Inc.	Nanoparticle coatings for flexible and/or drawable substrates

2006
- 2006-11-21 US US11/562,069 patent/US8138262B2/en active Active
2007
- 2007-11-07 PL PL07864024T patent/PL2091976T3/pl unknown
- 2007-11-07 PL PL12005942T patent/PL2527372T3/pl unknown
- 2007-11-07 CN CN200780046657XA patent/CN101563370B/zh active Active
- 2007-11-07 MY MYPI20092070A patent/MY145781A/en unknown
- 2007-11-07 EP EP12005942.3A patent/EP2527372B1/en active Active
- 2007-11-07 KR KR1020097012742A patent/KR101116435B1/ko not_active Expired - Fee Related
- 2007-11-07 NZ NZ577082A patent/NZ577082A/en not_active IP Right Cessation
- 2007-11-07 WO PCT/US2007/083892 patent/WO2008063887A2/en not_active Ceased
- 2007-11-07 CA CA2670055A patent/CA2670055C/en not_active Expired - Fee Related
- 2007-11-07 AU AU2007323973A patent/AU2007323973B2/en not_active Ceased
- 2007-11-07 EP EP07864024.0A patent/EP2091976B1/en active Active
- 2007-11-07 BR BRPI0717662-7A2A patent/BRPI0717662A2/pt not_active IP Right Cessation
- 2007-11-16 AR ARP070105113A patent/AR064255A1/es unknown
- 2007-11-20 TW TW096143969A patent/TWI424032B/zh not_active IP Right Cessation
- 2007-11-21 CL CL200703339A patent/CL2007003339A1/es unknown
2009
- 2009-06-08 NO NO20092204A patent/NO20092204L/no not_active Application Discontinuation
2012
- 2012-02-10 US US13/370,683 patent/US20120142818A1/en not_active Abandoned

Also Published As

Publication number	Publication date
CN101563370B (zh)	2013-03-20
EP2527372A1 (en)	2012-11-28
EP2091976A2 (en)	2009-08-26
WO2008063887A3 (en)	2008-08-14
EP2527372B1 (en)	2021-05-26
CN101563370A (zh)	2009-10-21
PL2091976T3 (pl)	2021-08-16
AR064255A1 (es)	2009-03-25
KR20090086601A (ko)	2009-08-13
BRPI0717662A2 (pt)	2014-02-25
AU2007323973A1 (en)	2008-05-29
NO20092204L (no)	2009-08-14
AU2007323973B2 (en)	2010-06-10
TW200837158A (en)	2008-09-16
US20080139708A1 (en)	2008-06-12
MY145781A (en)	2012-04-30
WO2008063887A2 (en)	2008-05-29
US20120142818A1 (en)	2012-06-07
EP2091976B1 (en)	2021-05-05
TWI424032B (zh)	2014-01-21
HK1135419A1 (en)	2010-06-04
KR101116435B1 (ko)	2012-03-07
US8138262B2 (en)	2012-03-20
CL2007003339A1 (es)	2008-07-04
PL2527372T3 (pl)	2021-10-04
NZ577082A (en)	2012-01-12
CA2670055A1 (en)	2008-05-29

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2021-10-12	MKLA	Lapsed	Effective date: 20210831
2022-10-07	MKLA	Lapsed	Effective date: 20191107

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